Handy Solutions Instant Hand Sanitizer with Aloe & Vitamin E

Handy Solutions Instant Hand Sanitizer with Aloe & Vitamin E

Drug Labeling and Warnings

Drug Details

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HANDY SOLUTIONS INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E- alcohol liquid 
Navajo Manufacturing Company Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Handy Solutions Instant Hand Sanitizer with Aloe & Vitamin E

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

  • A hand sanitizer to help reduce bacteria on the skin
  • A hand and lower arm sanitizer to help reduce bacteria on the skin

Warnings

Warnings   For external use only

Flammable. Keep away from fire or flame or sparks

When using this product do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears on the skin.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Place enough to cover both hands in the palm, and rub hands together until dry.
  • Children under 6 years of age should be supervised by  adult when applying this product.
  • Open cap. Place a small amount (enough to cover both hands) in the palm of your hand.
  • Rub hands together, spreading the sanitizer and rubbing vigorously until dry

Other Information

  • Store below 110 degrees F (43 degrees C)
  • May discolor certain fabrics or surfaces.

Inactive Ingredient

Purified water, triethanolamine, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, carbomer, aloe barbadensis leaf juice, fragrance.

Questions or comments?

Call toll-free 1-800-525-5097

or visit is on the web at www.navajomfg.com


Package Labeling

Hand Sanitizer Bottle LabelCarded Handy Solutions Hand Sanitizer

HANDY SOLUTIONS INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 67751-085
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 67751-085-021 in 1 PACKAGE10/28/2011
159 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC: 67751-085-0359 mL in 1 BOTTLE; Type 0: Not a Combination Product10/28/2011
3NDC: 67751-085-0430 mL in 1 BOTTLE; Type 0: Not a Combination Product10/28/201101/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/01/2011
Labeler - Navajo Manufacturing Company Inc. (091917799)
Establishment
NameAddressID/FEIBusiness Operations
Navajo Manufacturing Company Inc.136941411repack(67751-085)
Establishment
NameAddressID/FEIBusiness Operations
Ningbo Pulisi Daily Chemical Products Co., Ltd.529047265manufacture(67751-085)

Revised: 11/2019
 
Navajo Manufacturing Company Inc.


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